Analysis of genetic mutations in patients with hereditary angioedema (HAE) type I identified one family with novel homozygous mutation indicating rare instance of autosomal recessive inheritance

Kesim, B.Buyukozturk, S.Gelincik, A.Eraslan, S.Uzumcu, A.Mete, N.Sin, A.Ozseker, F.Erdenen, F.Colakoglu, B.Dal, M.Uyguner, O.2019-10-272019-10-2720080105-4538https://hdl.handle.net/11454/4076627th Congress of the European-Academy-of-Allergology-and-Clinical-Immunology -- JUN 07-11, 2008 -- Barcelona, SPAINeninfo:eu-repo/semantics/closedAccessAnalysis of genetic mutations in patients with hereditary angioedema (HAE) type I identified one family with novel homozygous mutation indicating rare instance of autosomal recessive inheritanceConference Object63340340WOS:000256235600906Q1